methyl 3-O-benzyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside

Base Information

Chemical Name:methyl 3-O-benzyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside
CAS No.:280569-49-5
Molecular Formula:C₂₂H₁₉Cl₄NO₇
Molecular Weight:551.207
Hs Code.:

Synonyms:methyl 3-O-benzyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside

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Chemical Property of methyl 3-O-benzyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside

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Technology Process of methyl 3-O-benzyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside

There total 4 articles about methyl 3-O-benzyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 77.0%

: 280569-45-1
methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside

: 280569-49-5
methyl 3-O-benzyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.5h;
DOI:10.1080/07328300008544079

Reference yield:

: 117-08-8
tetrachlorophthalic anhydride

: 280569-49-5
methyl 3-O-benzyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 54 percent / DIPEA / CH₂Cl₂ / 4 h / Heating

2: 77 percent / aq. TFA / CH₂Cl₂ / 0.5 h / 20 °C

With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; 1: Condensation / 2: Hydrolysis;
DOI:10.1080/07328300008544079

Reference yield:

: 280569-43-9
methyl 2-amino-3-O-benzyl-4,6-O-benzylidene-2-deoxy-α-D-altropyranoside

: 280569-49-5
methyl 3-O-benzyl-2-deoxy-2-tetrachlorophthalimido-α-D-altropyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 54 percent / DIPEA / CH₂Cl₂ / 4 h / Heating

2: 77 percent / aq. TFA / CH₂Cl₂ / 0.5 h / 20 °C

With N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; In dichloromethane; 1: Condensation / 2: Hydrolysis;
DOI:10.1080/07328300008544079